Cytochrome P450–catalyzed L-tryptophan nitration in thaxtomin phytotoxin biosynthesis

Nat Chem Biol. 2012 Oct;8(10):814-6. doi: 10.1038/nchembio.1048.

Abstract

Thaxtomin phytotoxins produced by plant-pathogenic Streptomyces species contain a nitro group that is essential for phytotoxicity. The N,N'-dimethyldiketopiperazine core of thaxtomins is assembled from L-phenylalanine and L-4-nitrotryptophan by a nonribosomal peptide synthetase, and nitric oxide synthase-generated NO is incorporated into the nitro group, but the biosynthesis of the nonproteinogenic amino acid L-4-nitrotryptophan is unclear. Here we report that TxtE, a unique cytochrome P450, catalyzes L-tryptophan nitration using NO and O(2).

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Biocatalysis
  • Cytochrome P-450 Enzyme System / metabolism*
  • Indoles / metabolism*
  • Nitric Oxide / metabolism*
  • Piperazines / metabolism*
  • Plants / microbiology*
  • Streptomyces / metabolism*
  • Tryptophan / metabolism*

Substances

  • Indoles
  • Piperazines
  • thaxtomine A
  • thaxtomine B
  • Nitric Oxide
  • Tryptophan
  • Cytochrome P-450 Enzyme System